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The product is an orthopedic planning solution for hip, knee, shoulder, hand, leg, or spine surgery.
December 2, 2019
By: mediCAD Hectec GmbH
mediCAD Hectec GmbH has reached another milestone in the internationalization of its mediCAD brand. Since earlier this fall, mediCAD with its 2D and 3D modules has been approved as a medical device for the Japanese market. mediCAD is a worldwide known orthopedic planning solution for hip, knee, shoulder, hand, leg or spine surgery. Manual and automatic dimensioning, integrated implant templates, archiving of required information and a traceability of findings in the preparation of operations and aftercare, make mediCAD demonstrably a software program with a high degree of planning and operation quality. With the approval of mediCAD as a medical device for the Japanese market as well as the recently closed sales partnership with TOYO Corporation, the company is now able to professionally and locally support hospitals and medical facilities in improving and digitizing the Japanese healthcare system. The growing interest and need for digital planning software in Japan have increased dramatically in recent years and months. “With this approval, we now expect a clear demand for our product as well as an increase in growth on the Japanese market. We look forward to this new challenge,” stated Jörn Seel, managing director of mediCAD Hectec GmbH. mediCAD is officially approved as medical device in roughly 30 countries inside and outside Europe. All European countries have approval and beside Japan, the company is allowed to sell mediCAD in the United States, Brazil, and Russia. “And we are continuously working on further country approvals such as e.g., South Africa or China,” said Seel.
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